336607-95-5

Basic information

• Product Name: 2,3-DIHYDRO-7-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YL)THIENO[3,4-B][1,4]DIOXINE-5-CARBALDEHYDE
• Synonyms: 2,3-DIHYDRO-7-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YL)THIENO[3,4-B][1,4]DIOXINE-5-CARBALDEHYDE
• CAS NO: 336607-95-5
• Molecular Formula: C₁₃H₁₀O₅S₂
• Molecular Weight: 310.3455
• Mol File: 336607-95-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 517.762°C at 760 mmHg
• Flash Point: 266.933°C
• Appearance: /
• Density: 1.528g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.67
• CAS DataBase Reference: 2,3-DIHYDRO-7-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YL)THIENO[3,4-B][1,4]DIOXINE-5-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIHYDRO-7-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YL)THIENO[3,4-B][1,4]DIOXINE-5-CARBALDEHYDE(336607-95-5)
• EPA Substance Registry System: 2,3-DIHYDRO-7-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YL)THIENO[3,4-B][1,4]DIOXINE-5-CARBALDEHYDE(336607-95-5)

Safety Data

• Hazardous Substances Data: 336607-95-5(Hazardous Substances Data)

Usage

Chemical structure

The compound has a complex structure with two thieno[3,4-b][1,4]dioxine rings, a 2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl group, and a carbaldehyde functional group.

Molecular arrangement

The compound has an intricate molecular arrangement, which likely contributes to its unique properties and potential applications.

Potential applications

Due to its unique structure and properties, the compound may have potential applications in the development of pharmaceuticals, plastics, polymers, or other materials.

Further research needed

Further research and analysis are necessary to fully understand the characteristics and potential uses of this chemical.

Molecular weight

The molecular weight of this compound is approximately 308.35 g/mol.

Appearance

The appearance of this compound is not specified in the material provided, but it is likely a solid or a viscous liquid.

Solubility

The solubility of this compound is not specified in the material provided, but it may be soluble in organic solvents such as ethanol or acetone.

Stability

The stability of this compound is not specified in the material provided, but it may be sensitive to heat, light, or moisture.

Reactivity

The reactivity of this compound is not specified in the material provided, but it may react with reducing agents, oxidizing agents, or other chemicals that can interact with its functional groups.

InChI:InChI=1/C13H10O5S2/c14-5-8-10-11(18-4-3-17-10)13(20-8)12-9-7(6-19-12)15-1-2-16-9/h5-6H,1-4H2

Upstream product

• 68-12-2 N,N-dimethyl-formamide 
• 195602-17-6 2,2'-bis(3,4-ethylenedioxythiophene) 

Downstream Products

• 336608-00-5 5-[(E)-(4-N,N-dimethylaminobenzylidene)methyl]-2,2'-bis(3,4-ethylenedioxythiophene) 
• 336608-05-0 5-formyl-5'-[(E)-(4-N,N-dimethylaminobenzylidene)methyl]-2,2'-bis(3,4-ethylenedioxythiophene) 
• 1159379-08-4 2-{5-[p-(di-p-tolylamino)styryl]-3,4-ethylenedioxythiophene-2-yl}-3,4-ethylenedioxythiophene 

Relevant articles and documents

Synthesis of π-conjugated 2,2:6′,2″-terpyridine-substituted oligomers based on 3,4-ethylenedioxythiophene

Dissymmetric π-conjugated monomers and oligomers incorporating 3,4-ethylenedioxythiophene (EDOT) units and bearing terpyridine end groups were synthesized in good yields through Vilsmeyer-Haak formylation followed by a reaction with 2-acetylpyridine in ba

Push-pull chromophores based on 2,2′-bi(3,4-ethylenedioxythiophene) (BEDOT) π-conjugating spacer

Replacement of 2,2′-bithiophene by BEDOT in push-pull NLO-phores produces a red shift of the absorption maximum accompanied with a large increase of the quadratic nonlinear optical susceptibility.